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Ion

FDA UDI

Class II (US FDA UDI)

by Intuitive Surgical, Inc.

Identity

Trade Name
Ion FDA UDI
Generic Name
Flexible video bronchoscope, single-use FDA UDI
Device Name
Vision Probe FDA UDI
Model / Reference
490106 FDA UDI
Description
Vision Probe FDA UDI

Identifiers

Primary DI / UDI-DI
00886874116128 FDA UDI
FDA Product Code
EOQ FDA UDI
GMDN Term
Flexible video bronchoscope, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
874.4680 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Flexible video bronchoscope, single-use

Ion by Intuitive Surgical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Flexible video bronchoscope, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 31df6c87-e411-43e1-b2e2-f3fec667e219 33 fields · synced Jun 9, 2026